358753-30-7

Basic information

• Product Name: 1,2,3,4,5,6,7,8-OCTAPROPYLANTHRACENE
• Synonyms: 1,2,3,4,5,6,7,8-Octapropylanthracene
• CAS NO: 358753-30-7
• Molecular Formula: C38H58
• Molecular Weight: 0
• Mol File: 358753-30-7.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2,3,4,5,6,7,8-OCTAPROPYLANTHRACENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4,5,6,7,8-OCTAPROPYLANTHRACENE(358753-30-7)
• EPA Substance Registry System: 1,2,3,4,5,6,7,8-OCTAPROPYLANTHRACENE(358753-30-7)

Safety Data

• Hazardous Substances Data: 358753-30-7(Hazardous Substances Data)

Usage

Chemical class

Polycyclic aromatic hydrocarbons (PAHs)

Derived from

Anthracene, a three-ringed aromatic hydrocarbon

Structure

Eight propyl groups attached to the carbon atoms of the anthracene molecule

Common uses

a. Precursor in the synthesis of organic materials
b. Production of various industrial products
c. Organic electronic devices (OLEDs, organic solar cells, and organic field-effect transistors)

Environmental impact

Considered an environmental pollutant

Health hazards

Potential human health hazard due to carcinogenic and mutagenic properties

Regulatory considerations

Use and handling should be carefully regulated to minimize exposure risks

Upstream product

• 358753-31-8 1,2,3,4,5,6,7,8-octapropyl-9,10-dihydroanthracene 
• 1942-45-6 4-Octyne 
• 636-31-7 1,2,4,5-tetraiodobenzene 
• 390409-94-6 1,2,3,4-tetrapropyl-6,7-diiodonaphthalene 
• 20485-44-3 2,3-dimethyl-2,3-diaminobutane 
• 74-88-4 methyl iodide 

Relevant articles and documents

Pd-catalyzed reactions of o-diiodoarenes with alkynes for aromatic ring extension

(Equation Presented) A new and efficient palladium-catalyzed reaction of o-diiodoarenes with internal alkynes produces naphthalenes or anthracenes in good to excellent yields. This procedure provides a simple, catalytic, and straightforward ring-extension method for constructing substituted polycyclic aromatic compounds.

Synthesis of acenes via coupling of 1,4-dilithiobutadienes with diiodoarenes in the presence of CuCl

Dilithiobutadienes prepared from diiodobutadienes reacted with diiodobenzene or diiodonaphthalene to afford substituted naphthalene, anthracene, dihydronaphthacene, and dihydropentacene derivatives in the presence of CuCl and DMPU. Dihydronaphthacene and

Polyacene derivatives and production thereof

The present invention relates to polyacene derivatives represented by general formula (I) below: (wherein R1 to R10, etc. each represents hydrogen atom, hydrocarbon group, or an alkoxy group; A1 and A2 are hydro

Aromatization of highly alkyl-substituted dihydroanthracenes using n-BuLi/TMEDA/MeI

Aromatization of highly alkyl-substituted dihydroanthracene was performed with the n-BuLi/TMEDA/MeI. Treatment of 1,2,3,4,5,6,7,8-octapropyl-9, 10-dihydroanthracene with 2.2 equiv of n-BuLi, TMEDA at 50 °C in hexane for 3 h, followed by 1.1 equiv of MeI at room temperature for 1 h gave the corresponding anthracene in 98% yield.